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Their mission is to promote early detection of brain aneurysms by providing knowledge and raising awareness of the signs, symptoms and risk factors. Work with the medical communities to provide support networks for patients and families, as well as to further research that will improve patient outcomes and save lives.

The Seeing Eye is a philanthropic organization whose mission is to enhance the independence, dignity and self-confidence of blind people through the use of Seeing Eye dogs.

RSRT was launched in 2008 to drive research toward a cure for Rett Syndrome and related MECP2 disorders. Our mission is urgent: 15,000 girls and women in the United States and 350,000 globally live with the agonizing symptoms of Rett Syndrome.

We exist to train local Community Health Workers with basic health knowledge and skills to improve the health of their own communities. Our vision is the end of preventable diseases in underprivileged areas globally by Educating, Empowering, and Equipping local health leaders, whose impact will change the course of their community.

The core mission of the IRSF is to fund research for treatments and a cure for Rett syndrome while enhancing the overall quality of life for those living with Rett syndrome by providing information, programs, and services. In 1983, a small dedicated group of parents whose children had Rett syndrome formed the first non-profit to focus exclusively on Rett syndrome – International Rett Syndrome Association (IRSA). In 2007, IRSA and Rett Syndrome Research Foundation (RSRF) consolidated resources to better serve families and maximize research investments toward a cure. The International Rett Syndrome Foundation (IRSF) emerged with a mission to accelerate research and empower families that builds upon these foundations’ pioneering work toward care and cure. We are walking this journey with you. IRSF is comprised of parents and friends of those diagnosed with Rett syndrome. We are dedicated to empowering families with the latest medical information, offering meaningful support and resources, and advocating for all those living with Rett syndrome. Our strategy is simple but powerful: improve care today and create treatments for tomorrow. IRSF is committed to a full-spectrum approach, providing solutions for everyone living with Rett syndrome. We do this by investing in innovative research, working to build a robust treatment pipeline, and removing barriers to ensure clinical trial success.

National Breast Cancer Foundation's (NBCF) mission is to save lives through early detection and to provide mammograms for those in need.Our mission includes increasing awareness through education, providing diagnostic breast care services for those in need, and providing nurturing support services.

Every Mother Counts is a non-profit organization dedicated to making pregnancy and childbirth safe for every mother. They inform, engage, and mobilize new audiences to take actions and raise funds that support maternal health programs around the world.

Prime of life neurodegeneration is a spectrum of relatively rare diseases that often afflict people during productive, active years and lead to debilitating symptoms and early death. They are generally categorized as frontotemporal disorders and are characterized by progressive personality, behavior, language and motor decline. These diseases create a level of functional impairment that significantly compromises the ability to carry out activities of daily living. There is currently no treatment and no cure, but there is hope. Research into these diseases may be a gateway to understanding and ultimately preventing, treating and curing more common neurodegenerative diseases like Alzheimer's and Parkinson's. CurePSP is the leading organization within this disease spectrum, providing support for patients, families and caregivers; awareness and education to healthcare professionals; and global research funding. Current research into prime of life diseases, especially progressive supranuclear palsy (PSP), is showing great promise for unlocking the secrets of neurodegeneration.

Join Bridge to Türkiye Fund, where we connect grassroots communities around the world for a brighter Türkiye—transforming goodwill into impactful programs that improve lives. A culture of giving and civic involvement is a part of our heritage. Bridge to Türkiye Fund (BTF) was founded in 2003 by a few like-minded Turkish-Americans and friends of Türkiye with the simple desire to give back. BTF is founded on citizen-based, democratic and secular principles and encourages all to contribute to the educational welfare of less fortunate children in Türkiye. Based in the Triangle area of North Carolina, BTF grew all across the US over two decades, with many regional giving circles, and today has individual donors and supporting communities in all parts of the globe. Our focus areas are: Enabling equality and equity in education Improving physical and mental health with an emphasis on future generations Disaster relief, recovery and resilience Preservation of natural life and enivronmental sustainability Our simple and shared vision is to unite people and give back as a community. It is an organized attempt to leverage individual diaspora resources who believe in the power of investing together for education and building better futures for disadvantaged youth in Türkiye. BTF maintains a portfolio of carefully vetted Turkish NGOs and localized projects to accomplish its mission. This makes it possible for BTF’s donors to support great causes simply and safely from abroad. For more information, visit our website or reach out at: info@bridgetoturkiye.org.

National Brain Tumor Society is fiercely committed to finding better treatments, and ultimately a cure, for people living with a brain tumor today and anyone who will be diagnosed tomorrow. This means effecting change in the system at all levels.

We are honored to provide resources and support to the millions of people living with Alzheimer's disease and to their families, friends and caregivers who support them on a daily basis. If you or someone in your family has been diagnosed with Alzheimer's disease or another form of dementia, we are here to help. You can get free, confidential counseling and support today. The End Alz Association is proud to be a leader in the fight to #EndAlz but we couldn't do it without your support. Please join us and make a donation today. Together, we can #EndAlz!

For more than 20 years, the Clinton Foundation has transformed philanthropy — running programs that develop leaders and accelerate solutions to the world’s most pressing challenges. Under the leadership of President Clinton, Secretary Clinton, and Chelsea Clinton, our unique approach prioritizes solutions over ideology — bringing people together in the spirit of collaboration and pragmatic problem-solving for a brighter future. Programs founded by the Clinton Foundation since its inception reflect our shared commitment to “putting people first” — the practice of focusing on how a proposed policy, program, or partnership can directly affect a person’s life and make a lasting impact.